Our Validated Migration Process
Minimize risk and ensure regulatory compliance during your pharmacovigilance system transition
Compliance-Focused Features
Our migration methodology incorporates essential pharmacovigilance requirements
Bidirectional Traceability
Maintain complete audit trails from source to target system with full case history preservation.
Data Integrity
ALCOA+ principles applied throughout migration process with checks for completeness and accuracy.
Global Compliance
Support for regional requirements including EU GVP, FDA 21 CFR Part 11, and Japan PMDA standards.
Historical Data Preservation
Migration of complete case histories including amendments, follow-ups, and regulatory correspondence.
MedDRA/WHO-DD Version Management
Handling of coding changes across different dictionary versions during migration.
Role-Based Access Control
Maintenance of user permissions and access levels during system transition.
Expert pharmacovigilance solutions to safeguard patients, ensure compliance, and drive innovation in drug safety. Partner with us for precision, vigilance, and regulatory excellence.
India
India - Headquarters
Pristine City Bakori Road, Wahgoli, Pune, Maharashtra - 412207
+91 90283 33221
India - Development Center
Baba Somnath Tower, Bypass Ramur Road, TP Nagar Haldwani Uttarakhand 263139
+91 90283 33221
Australia
Australia Office
ACN: 664 913 928
38 Energy Dr lyndhurst VIC 3975, Australia
38 Energy Dr lyndhurst VIC 3975, Australia
+61 4 0461 3093